IL44362A - Process for the production of microcapsules - Google Patents

Description

ηιτντ morns ηιχ»»1» T»*?nn Process for the production of microcapsules BAYER AKTIENGESELLSCHAFT C. 42338 .

This invention relates to a process for the production of microcapsules.

The microencapsulation of organic and inorganic substances is already known in principle. It can be carried out, for example, by a process of interface polycondensatiori in which two low molecular weight reactants are dissolved in different liquids which are immiscible with each other, the two solutions are added together and the reactants react with each other at the interface to form a polymer (see. U.S. Patent Specifications No. 3 , 575,882; 3 , 577 , 515 and 3 , 607 , 776 ) .

In practice, microencapsulation is carried out by first preparing a stable emulsion in which the disperse phase comprises the material which is to be encapsulated and the solution of one of the low molecular weight reactants in a solvent and the continuous phase comprises a liquid which is immiscible with these substances. The preparation of this emulsion generally requires the use of emulsifying agents.

The second reactant, dissolved in an organic solvent, is added to this emulsion. Envelopes consisting of the polymer formed by the reaction between the reactants are formed over a period of time, usually several hours, round the dispersed particles of the material which is to be encapsulated. Suitable pairs of reactants for this process are, for example, diisocyanates/diols; diisocyanates/diamines; dicarboxylic acid chlorides/diamines; disulphonyl chlorides/diamines or phosgene/diamines .

Encapsulation processes of the kind described above have several important disadvantages, one of which is that a stable emulsion must first be prepared. This is often difficult, i ll inc i n c s is sufficiently stable so that it will not break down when the second component is added. Furthermore, there is little scope for variation of these processes because there is 'only a narrow, choice of suitable reactants and the polymers which can be produced in this way are few . in number and very similar to each other. Moreover, the low molecular weight reactants used are practically incapable of film formation and it is therefore necessary to use a! large quantity of enveloping material for encapsulation. This means that only a small quantity of core material can be encapsulated in a large quantity of enveloping material.

It is known from British Patent 1,091,076 to first prepare a hydrophobic solution of, for instance, a polyisocyanate, then to prepare a hydrophilic solution of a material reactive with the isocyanate (for instance, a polyol) , then disperse the second, solution in the first and start the polyaddition reaction. For the reaction according to British Patent 1,091,076 the use of a polar solvent and the formation of a stable dispersion is necessary. In contrast thereto the process according to the present invention does not require the formation of stable dispersions and requires no polar solvent. Core materials and film forming materials are directly emulsified into the continuous liquid phase under high turbulence.

It is thus an object of this invention to provide a new proc for the production of microcapsules which is characterised in that a reaction product of a diol or polyol which has a molecular weight of 400 to 10,000 with phosgene or a di isocyanate or polyisocyanate which contains at least two chloroforinic acid ester* or isocyanate groups per molecule is mixed with the material which is to be enveloped (core material), and the resulting mixture, a chain lengthenin agent which is at least bifunctional and an aqueous phase are introduced into a zone of high turbulence in which the reaction product and chain lengthening agent reaot together to form a high molecular weight polymer which envelops the core material to form microcapsules are then separated. The reaction products of idioljs or polyols with diisocyanates or polyisocyanates which still contain isocyanate groups will hereinafter be referred to as "isocyanate prepolymers" and the corresponding reaction products with phosgene will be referred to as "chloroformic acid ester prepolymers".

This process has important commercial advantages; in particular, the separate preparation of a stable emulsion is no longer necessary. Instead, an emulsion is prepared inthe zone of high turbulence and this emulsion already undergoes reaction during its preparation and immediately thereafter.

The whole time required for the production of the microcapsules is only a few seconds or, at the most, a few minutes.

Moreover, the process is generally continuous so that maximum volume/time yields can be obtained. With the process according to the invention it. is also possible to encapsulate substances which are sensitive to temperature and substances which are readily hydrolysed or oxidised because the process can be carried out at a low temperature and high velocity. The reaction products of diols or polyols with phosgene or with diisocyanates or polyisocyanates are generally film-forming so that only small quantities of enveloping material compared with the core material are required. Lastly, the properties of the enveloping material can be varied within very w.ide limits, for example hydrophilic envelopes are obtained by using a polyether with a high proportion of ethylene oxide units as the polyol with a molecular weight of 400 to 10,000 whereas envelopes which are easily degraded hydrolytically can be obtained, for example, by using polyesters of oxalic acid, malonic acid or succinic acid; envelopes which can be degraded by oxidation and envelopes with varying degrees of hardness and practically any desired melting range can be obtained by other suitable choice of starting materials.

Particularly suitable reaction products of diols or polyols with phosgene or di- or polyisocyanates are obtained b reacting linear or branched polyols with excess quantities of isocyanate or phosgene, polymers which contain terminal ■frepcyanate or chlorocarbonyl groups being then obtained.

^ Polyole suitable for preparing the reaction products have a molecular weight of 400 to 10,000 preferably.1000 to 10,000 to 10,000 and contain from 2 to 8 hydroxy1 groupe per molecule. PolyesterB, polyethers, pol hioethere , polyacetals, polycarbonates and polyester amides are particularly suitable.

Suitable polyesters are obtained, for example, by reacting polyhydric alcohols, preferably dihydric alcohols optionally with the addition of trihydric alcohols, with polybasic, preferably dibasic, carboxylic acids. Instead of the free polycarboxylic acids, the corresponding polycarboxylic acid anhydrides or corresponding polycarboxylic acid esters of lower alcohols or mixtures thereof may be used for preparing the polyesters. The polycarboxylic acids may be aliphatic, cycloaliphatic , aromatic and/or heterocyclic and may be substituted, e.g. with halogen atom, and/or unsaturated.

The following are mentioned as examples: Succinic acid, adipic acid, suberic, azelaic acid, sebacic acid, }jhthalic acid, isophthalic acid, trimellitic acid, phthalic acid anhydride, tetrahydrophthalic acid anhydride, h.exahydrophthalic acid, anhydride , tetrachlorophthalic acid anhydride, eiidouiethyl- ene tetrahydrophthalic acid anhydride, glutaric acid anhydride, maleic acid, maleic acid anhydride, fumaric acid, dimeric and trimeric fatty acids such as oleic acid optionally mixed with luonomeric fatty acids, dimethylterephthalate and bis-glycol terephthalate. The following are examples of polyhydric alcohols which may be used: ethylene glycol, propylene- 1.2- and -1,3-glycol, butylene-1 , - and -2,3-glycol, hexane-1,6-diol, octane-1 , 8-diol , neopentyl glycol, cyclohexane dimethanol ( 1 , 4-bis-hydroxymethylcyclohexane) , 2-inethyl-propane- 1.3-diol, glycerol, trimethylolpropane, hexane-1 , 2, 6-triol , butane-1 ,2,4-triol, -trimethylolethane, pentaerythritol, quinitol, manntol and."sorbitol, methylglyooside, diethylene glycol, triethylene glycol, tetraethyleneglycol, polyethylene glycols, dipropylene glycol, polypropylene glycols, dibutylene glycol and polybutylene glycols. The polyesters may also contain contains a proportion of terminal carboxyl groups. Polyesters of lactones such as £ -caprolactone or of hydroxycarboxylic acids such as i-hydroxycaprocji. acid may also he used.

Suitable polyethers containing from 2 to 8, preferably 2 or 3 hydroxyl groups may be prepared,, for example, by polymerising epoxides such as ethylene oxide, propylene oxide, butylene oxide, tetrahydrofuran, styrene oxide. or epichloro-hydrin, each with itself,. e..g. in the presence of BF^, or by addition of these epoxides either as mixtures of successively to starting components which contain reactive hydrogen atoms such as alcohols or amines, e.g. water, ethylene glycol, propylene-1,3- or -1 , 2-glycol , trimethylolpropane, dihydrpxy-diphenylpropane, aniline, ammonia, ethanolamine or ethylene diamine. Sucrose polyethers, e.g. those described in German Auslegeschriften No. 1^176,358 and 1, 064,938, may also be . used "for the process according to the invention.

It is frequently preferred to use those polyethers which contain predominantly primary hydroxyl groups (up to 90$ by weight, based on all the hydroxyl groups present. in the polyether).

Polyethers which have been modified with vinyl polymers, e.g. the modified polyethers obtained by the polymerisation of styrene or acrylonitrile in the presence of polyethers (U.S.

Patent Specifications No. 3,383, 351 ; 3,30^, 273 ; 3, 523 , 093- and 3,110,695 and German Patent Specification No. 1, 152,536) and polybutadienes which contain hydroxyl groups are also and pages 44 - 45 and Volume II, 1964, pages 5 - 6 and 198 and 199 and in Kunststoff-Hahdbuch, Volume VII^ Vieweg-HBchtlen, Carl-Hanser-Verlag Munich, 1966, e.g. on page» 45 to 71. The dilsooyanates or polylsocyanates used for the reaction with the polyole (to form the so-called isocyanate prepolymere) may be aliphatic, cyoloaliphatic, araliphatic, aromatic or heterocyclic polylsocyanates (see Ann. 562, pages 75 to 136), for example ethylene diisocyanate; tetramethylene-1 ,4-dlisooyanate; hexa-methylene-1 ,6-diisocyanate; dodecane--) i 12-diisocyanate; cyclobutane-i , 3-diisocyanate; cyclohexane-1 , 3-and -1, ^-diisocyanate arid an mixtures of these isomers; 1-i socyanato-3 , 3 , 5-trimethyi-5-i socyanatometliyl-cyclohexyne (German Auslegeschrift No. 1,202,685); hexahydrotolylene.-2 , k-and -2 , 6-diisocyanate and any mixtures of these isomers; hexahydrophenylene-1, 3- and/or 1 , '.-diisocyanate; perhydro-2, k % -and/or 4, '-diisocyanate; phenylene-1 , 3- and -1 , 4-diisocyanate; tolylene-2, 4-and -2,6-diisocyanate and any mixtures of these isomers; diphenylmethane-2, - and/or , V -diisocyanate; naphthylene-1 , 5-diisocyanate; triphenylmethane—¾, h f V-triiso-cyanate; polyphenyl-polymethylene polylsocyanates (obtained by aniline-formaldehyde condensation followed by phosgenation in accordance with British Patent Specification No; 87¾,¾30 and 8¾8,67l); perchlorinated aryl polylsocyanates (see German Auslegeschrift No.- 1,157,601); polylsocyanates which contain carbodiimide groups (see German Patent Specification No. 1,092,007); diisocyanates according to U.S. Patent Specification No. 3,^92,330; polylsocyanates which contain allophanate groups (see British Patent Specification No. 99^,890; Belgian Patent Specification No. 761,626 and Dutch Patent Application No. 7, 102, 2¾); polylsocyanates which contain isocyanurate groups (see German Patent Specifications No. 1,022,789; 1,222,067 and 1,027, 39V, German. Offenlegungsschriften No . 1,929,03* and 2,00 i,0i8) ; polyisocyanates which contain urethane groups (see Belgian Patent Specification No. 752,261 and U.S. Patent Specification No. 3,39¾fl6¾); polyisocyanates which contain acylated urea groups (see German Patent Specification No . 1 , 230 j778) ;· polyisocyanates which contain biuret groups (see German Patent Specification No.. 1,101,39* 5 British Patent Specification No. 889,050 and French Patent Specification No. 7,017,51*»); polyisocyanates which have been prepared by teloraerisation reactions (see Belgian Patent Specification No. 723,64ο); polyisocyanates which contain ester groups (see British Patent Specifications No. 956;½7*i and 1,072,956; U.S.

Patent Specification No . 3,567,763 and German Patent Specification No. 1,231,688) and reaction products of the above mentioned isocyanates with acetals (see German Patent Specification No. 1,072,385).

The preparation of isocyanate prepolymers from polyols and isocyanates is already known (see R.Vieweg, A.HOchtlen, Kunststoff-Handbuch," Volume VII, Polyurethane, Carl-Hanser- Verlag, Mxmich, 1966, pages 8*» and 85).

The isocyanate prepolymers may be used directly fo encapsulation in the form in which they are obtained in their preparation but the monomeric isocyanates still present in them may also be removed by a process of distillation, e.g. by thin layer evaporation.

Preparation of the chlproformic acid ester prepolymers is carried out in known manner by reacting the polyols with excess phosgene.. prepolymers and isoeyanate and chloroforiuic acid ester prepolyuiers may be aliphatic, cycloaliphatic or aromatic glycols or amino glycols which contain hydroxy1 groups or hydroxy1 and amino groups or aliphatic, cycloaliphatic.. or aromatic amines.

The " following are examples of siich compounds: Ethylene glycol, d.i ethylene glycol, triethylene glycol, propane-1,2- diol, propane-1 , 3-diol , dipropylene glycol, thiodiglyeol , hutane-1,2-, -1,3-, -2,3- and -1,4-diol, 3-chloropropane-l > - diol , pentane-1 , 5-dio.l , 2-methylpentaiic-2 , 4-diol , 3-'»ethyl om ar 2, -dioi , 2, 2-dimethylpropane-l , 3-diol, butane-2-cliol-( 1 , h ) , butyne-2-clio.l-( 1 , ) . hexane-2 , 5-diol , eye1ohcxanedi o1» , 1 , 6-diol , N-mcthylrdiethanol amine , N-ethyl-diethano amiuc: , diethanol amine , dii sopropanolamine , Ν,Ν· -bis-( 3-aminopropyl )-ethylenediamine, Ν,Ν' -bis-(2-aminopropyl) -ethyl enediamine, Ν,Ν' -bis-(2-aminoe thy1 ) -ethyl enedi mine, Ν,Ν' -bis-(2-aminopropyl ethylene diamine, N,N'-bis-(2-aminoethyl)-ethylenediamine, 4,4'-diraethylamino-diphenylmethane,. 4, 4' -dimethylamino-3, 3 ' -dimethyl-diphenylmethane, hexanetriol , s glycerol, triethanolamine , trimethylolpropane, pentaerythri tol , hydrazine and hydrazine derivatives, tris-(hydroxyalkyl)phosphites, glucose,, bisphenol A, 4, thane, 2, 4- and 2 6-diaminotoluene or addi tionproducte (molecular weights generally 200 to 1500) of alkylene oxides such as ethylene oxide, propylene oxide or butyleno oxide with low molecular weight compounds of this kind which contain active hydrogen atoms or with water.

The envelopes therefore contain urethane and/or urea groups in addition to the typical groups of the polymers siich as ether and ester bonds. In principle, any pair of reactants may be chosen but the choice will depend on the reactivity of Le A U 928 -9- the two components, for example when using prepolymers obtained from aliphatic isocanates which are slow to react, it is advisable to use aliphatic polyamines , which are highly reactive, whereas when using prepolymers obtained from highly active aromatic isocyanates it is advisable to combine these with less reactive compounds such as aromatic polyamines, glycols and aminoalcohols. The two reactants for producing the capsules may be used in quantities such that the reactive groups are present either in less than stoichiometric quantities. The reaction proceeds particularly rapidly if the cross-linking low molecular weight components are used in excess whereas envelops with exceptionally low melting ranges are obtained if these components are used in less than stoichiometric quantities.

The molar ratio of the reactive groups (isocyanates or chloroforinic acid ester groups on the one hand and active hydrogen of the chain lengthening agent on the other) is preferably between about 1:0.8 and 1:1.8; it is particularly advantageous to use a molar ratio of 1:1.

The reaction velocity can also be . influenced by the known catalysts used for polyurethane formation.

The following are examples of suitable catalysts: 1.) Tertiary amines such as triethylamine, tributylamine., N-methylmorpholine , N-ethyl-niorpholine , N-cocomorpholine, ,Ν,Ν' ,Ν' -tetraiuethyl-ethylenediamine, 1 , 2i-diaza-bicyclo-(2, 2, 2) -octane, N-methyl-N ' -dimethylaminoethyl-piperazine, Ν,Ν-dimethy1benzylamine, bis-(N,N-diethylaminoethyl )-adipate, N,N-diethy.lbenzylamine, pentamethyldiethylenetriamine, N, N-dimethylcyclohexylamine , Ν, ,Ν1 ,Ν' -tetramethyl-1 , 3-bu tane- diamine, N,N-dimethyl-fl-phenylethylamine, 1 , 2-dimethylimidazole and 2-methylimidazole ; diamine, N,N-dimethyl-P-phenylethylaiuine, 1 , 2-dimethylimidazole. and 2-7methylimidazble; 2. ) Tertiary amines containing hydrogen atoms which are reactive with isocyanate groups, e.g. triet anolamine, triisopropanolamine, N-methy 1-diethanolamine , N-ethyldiethylanol-amine, . N,N-dimethylethanolatnine and their reaction products with · alkylene oxides . such as propylene oxide and/or ethylene oxide; 3 . ) Silaamines which contain carbon-silicon bonds such as those described e.g. in German Patent Specification No. 1 , 229,290 e.g. 2 , 2 ,--trimethyl-2-silamorphoiine or 1 , 3-diethylaminOmetbyl-tetra-methyl-disiloxane; li. ) Bases which contain nitrogen, such as tetraalkylaniraonium hydroxides, alkali metal hydroxides such as sodium .hydroxide", alkali rife al phenolates such as sodium phenolate.or alkali me al, alcoliolatcs such as sodium methylate and hexahydro riazines 5 . ) Organic metal, compounds, in particular organic tin compounds, preferably tin(ll) salts of carboxylic acids such as tin(ll) acetate, tin(ll) octoate, tin(ll) ethylhexoate and tin(ll) laurate and the dialkyl tin salts of carboxylic acids, e.g. dibutyl tin diacetate, dibutyl tin dilaurate.,_dibutyl tin maleate or dioctyl tin diacetate.

Other catalysts and details of their, mode of action may be found in Kuhststoff-Handbuch, Volume VII, published by Vieweg and HOchtlen, . Carl-Hanser-Verlag Munich, 1966 , in particular on pages 9 to 102 .

The catalysts are generally used ih quantities of from 0 .001 to 10^ by weight, based on the reactants.

The process according to the invention may be used for encapsulation of any solid or liquid substances provided that they are insoluble in water and inert towards the prepolymers and chain lengthening agents. The following are examples of substances which may be encapsulated: Flame retarding agents such as tris-chloroethylphosphate or tris-(2, 3-dibrotno-propyl )- phosphate, catalysts such as Ν,Ν'-dimethylbenzylamine, tin(ll) octoate or dibutyl tin( IV) . dilaurate, aliphatic, cycloalipha ic or aromatic glycols, polyols used for the preparation of polyurethane foams and polyurethane elastomers, plasticizers such as dioctylphthalate, plant protective agents, perfumes, inks or aliphatic and aromatic hydrocarbons such as petroleum hydrocarbons or benzene.

The aqueous phases used are preferably water or aqueous emulsifier solutions. The emulsifiers, are generally used in quantities of from 0.1 to \ by weight. The quantity of aqueous phase, based on the prepolymer, is preferably from 50 to 80$ ■ by weight .

So-called laminators (see Belgian Patent Specification No. 718,029) may also be used either in combination with or instead of the emulsifiers. .

When carrying out the process of the invention, the substance which is to be.; encapsulated may first be dissolved or dispersed in the prepolymer, using μρ to 9 by weight of this substance, based on the quantity of prepolymer, preferably from 20 to 60# by weight. The process of dissolvin or - dispersing the material which is to be encapsulated can be facilitated by adding small quantities of water-soluble, inert organic solvents (e.g. acetone in quantities of 5 to 20$ by weight, based on the prepolymer) .

The chain lengthening agent may be partly or completely dissolved in the aqueous phase.

The mixture of prepolymer and material which is to he encapsulated, chain lengthening agent (if it is not dissolved in the aqueous phase) and the aqueous phase are then introduced separately from each other into the zone of high turbulence at a temperature at which all the reactants are liquid hut which is not above the decomposition temperature of the starting materials and of the chain lengthened polymer produced. In order to observe these conditions it is frequently necessary to operate at excess pressure, at least at a pressure above. the vapour pressure of the most volatile component. Temperatures of from 50 to 150°C are preferably employed.

The temperature in the zone of high turbulence should in any case be above. the melting point of the isocyanate prepolymer. Only then can products be obtained in the form of uniform spherical particles.

The zone of high turbulence in the context of this invention is generally a space through which at least 300 parts by volume of liquid are passed through fo each part by volume of space per hour under conditions of vigorous mixing. The quantity of liquid passed through for each part by. volume of the zone of turbulence per hour is preferably 1200 to 'k ; parts by volume.

The zone of high turbulence is generally produced with the aid of known apparatus, for example a stirrer vessel with disc. stirrer and flow breakers in which the ratio of the diameter of the vessel to the diameter of the stirrer is between 1:0.9 and 1:0.2. When this apparatus is used, separate introduction of the different components can be achieved by introducing one component (e.g. the aqueous phase plus chain lengthening agent) directly into the stirrer" cbne and the other component (e.g. the isocyanate prepolymer) into the hollow shaft of the stirrer so that the two components are rapidly emulsified and chain lengthening takes place in the already emulsified, product.

The mixing power in a vigorously agitated stirrer vessel is generally 10 —~1 to 10™~J Watt/cm and is higher i the stirrer, cone itself and therefore sometimes sufficient to emulsify low viscosity pr.epolymers .

Pumps equipped with rotors are much more suitable for carrying out the process, mainly because the time of stay is strictly limited. Exceptionally vigorous mixing can be achieved within very short times of stay in rotary horaogenization machines. These apparatus are therefore preferred. They have a very high rate of throughput. The specific mixing power of rotary homogenization' machines is about 5-25 The process may be carried out by introducing the prepolymer which contains the material which is to be encapsulate the chain lengthening agent and the .aqueous phase separately into the zone of turbulence. Alternat vely, two of these components, 'e.g. the aqueous phase and the chain lengthening agent, may be mixed. This is to be recommended particularly if the chain lengthening agent is water-rsoluble . If desired, the reactants may also be introduced at various points into the zone of turbulence and the stream of one component may be subdivided into several partial streams, for example the prepolymer which contains the material which is- to be encapsulated and the aqueous phase may be introduced at the beginning of the zone of turbulence and the chain lengthening agent may be introduced simultaneously at several points at the beginning, middle and/or end of the zone of turbulence.

According to one particularly advantageous method of carrying out the process, all three components are passed through a zone of decreasing temperature after they have been mixed.

Since the chain lengthening reaction takes place rapidly at high temperatures, it is advisable to employ high temperatures in the zone of turbulence. In order to operate the reaction continuously at its optimum conversion rate and for example to vary the particle size of the product, the zone of turbulence may be associated with additional zones of turbulence operated at decreasing temperatures. For example, the first zone of turbulence may be kept at a temperature above the melting point of the starting materials and of the polyu ethane produced while a following reaction zone may be kept at a temperature near the melting point of the polyurethane and of the prepolymer while a following cooling zone may be kept at a temperature below the softening temperature of the polyurethane or polyurethane urea. ' The polyaddition reaction may be stopped by washing the reaction mixture with acidified water.

The, process of the invention will now be described in more detail with reference to two figures. The term "isocyanate prepolymer" used below refers to the mixture of isocyanate prepolymer or chloroformic acid prepolymer and the material which is to be encapsulated.

Figure 1 shows an arrangement for carrying out the process. A mixing apparatus (1) is continuously supplied with an isocyanate prepolymer and the substance which is t'of be encapsulated from the storage tank (10) by way of the gear wheel pump (11) and valve (12 and at the same time with emulsifier and/or chain lengthening agen by way of piston delivery pumps (6+7), valves (5), mixing device ( heat exchanger (3) and non-return valve (2). The isocyanate A mixing apparatus (l) is continuously supplied with an isocyanate prepolymer and the substance which is to be encapsulated from the storage tank (lO) by wa of the gear wheel pump (ll) and valve (12) and at. the same time with emulsifier and/or chain lengthening agent. by way of piston delivery pumps (6+7),· valves (5), mixing device (k) , heat exchanger (3) and non-return valve (2). The isocyanate prepolymer is emulsified in the mixing apparatus (l), the prepolymer forming the disperse phase. of the emulsion. The chain lengthening reaction of the prepolymer is also carried out in this apparatus by the simultaneous addition of the chain lengthening agent. After preparation of the emulsion in the mixing apparatus (l), the emulsion is transferred to the reaction vessel (l½) by way of a pressure control valve (13) and pH meter (15).

The chain lengthening agent may also be introduced directly into the mixing apparatus (l) by way of the pump . (7a) and non-return valve (2a) or a part may be introduced along one path and a part along the other. The pH is the governing parameter' for coritrollong the reaction.

Figure 2 shows another apparatus for carrying out the-process. In this case, a mixing apparatus (6) is supplied simultaneously with isocyanate prepolymer and substance which is to be encapsulated from an extruder (17), with aqueous phase from the storage vessel (l) by way of a piston delivery pump (2), non-return valve (3) and heat exchanger ( ) and with chain lengthening agent from storage vessel (10) by way of piston delivery pump (8) and non-retur valve (5). The emulsion produced in the mixing apparatus (6 enters the . reaction tube of the heatin circuit (9). Part of the emulsion is recirculated from this tube into the mixing apparatus (6) and the remainder is transferred to the reaction tube of the cooling circuit (15) through the reducing aperture (l6).

Part of the contents of this tube is passed through the cooler (12) and rotary pump (H) to be cooled in the cooling circuit and part is discharged, through the tank (13). The whole plant is under the pressure of nitrogen which is introduced into the reaction tube ( 15) and tank (13) from the cylinder ' A dispersion of polymer particles which enclose the material which is required to be encapsulated is removed from the zone of turbulence of the apparatus described. The solid product can be isolated from these dispersions in the usual maimer, for example the- emulsion may be left to cream up, optionally in a centrifugal field, and the remaining water may then be removed in a conventional, drying apparatus, e.g. a shelf drier or flow, drier. A free flowing powder is then left, the particles of which envelop the material which is required to be encapsulated.

Le 14 928 -17- Examples I. Examples for preparing isocyanate prepolymers .

Method A ¾9.5 Parts by weight of hexamethylene-1 , 6-diisocyanate are added to 160.5 parts by weight of a trifunctional polyether of trimethylolprppane and propylene oxide which has a molecular weight of 300 and a hydroxyl number of 6 and the mixture is heated to a temperature of between 100°C and 105°C for 2.5 hours; A prepoly mer which has an isocyanate group content of 9.3$ and a viscosity of 700 centipoises at 25°C is formed. Method B 622 Parts by weight of hexamethy ene-1 , 6-diisocyanate are added to 378 parts by weight of a trifunctional polyether of trimethylolpropane and propylene oxide which has a molecular weight of i¾50 and a hydroxyl number of 375 and jthe mixture is heated to a temperature of between 100°C and 1Q5°C for 5 hours. A prepolymer which has an isocyanate content of 17.3# has been formed at the end of this time.

Method C 339 Parts by weight of a trifunctional polyether of glycerol, propylene oxide and ethylene oxide which has a molecular weight of 6000 and a hydroxyl number of 28 are mixed with ¾6l parts by weight of hexamethylene-1, 6-diisocyanate and the mixture is heated to a temperature of between 100°C and 105C for 5 hours. A liquid prepolymer with an isocyanate content of 21$ has formed by the end of this time.

Method D ¾59.2 Parts by weight of a hexafunctional polyether of sorbitol, propylene oxide (77$ by weight) and ethylene oxide I j (23$ by weight) which has a molecular weight of 14000 and a diisocyanate . The mixture is heated to a temperature of 120 C or 6 hours. By the end of this time, a prepolymer which has an isocyanate content of 20 . 1 and a viscosity of 3^3 centipois j at 25°C has been formed.

II. Examples for encapsulation.

General description (apparatus shown in Figure l) 180 kg/h of a mixture of isocyanate prepolymer and substance which is required to be encapsulated are supplied from the storage vessel (10) to the mixing apparatus (Supraton D 205 , output 2000 l/h) . At the same time, 700 1 per hour of water from vessel (9 ) and a 20$ by weight diamine solution from vessel (8) are supplied to the mixing apparatus by way of pumps ( 7 ) and ( 6 ) and mixer (½). 'The quantity of, diamine used is calculated to adjust the molar ratio of amine groups to isocyanate groups to the required value. This ratio is defined by constants. The constant is obtained from the formula , mols of amino groups χ mols of isocyanate groups An aqueous dispersion of the capsules formed is removed from the mixing apparatus through valve ( 13 ) and collected in vessel ( 4). The dispersion may be freed from water in a fluidised bed drier. The capsules are then obtained in the form of a dry powder.

The experiments described above are summarized in the following table: f CD to of 00 Experi?re- CO content EncapAmine Constant r'olymer ment poly- % by v/eight sulated % hy No. mer subweight stance 1 A 9.3 . a SDA 20 70 2 B 9.3 b EDA 130 20 3 B 17.3 a EDA 100 30 4 A 9.3 c ED 100 70 ? - A 9.3 d EDA 100 70 IV) 6 C 21 c EAS 1C0 30 7 C 21 d EAS 100 30 8 c 21 e EAS 1 10 40 9 c 21 f EDA 120 20 10 c 21 c EDA 1 10 50 1 1 c 21 d - EDA 1 10 50 12 D 20. 1 S EAS 80 70 13 — —B CXJ · 11 _1) —EAS 100 30 EDA » ethylene diamine EAS ■«= ethylene diaminosulphonic acid sodium a leather perfume b » mineral oil c <= (diethoxy-thiophosphoryl-oximino)-phenyl-acetonitrile d = 0, 0-dimethyl-0-( -nitrophenyl) -thiophosphat e e «= N-dichl'orofluoromethylthio-(dimethyl-sulphonamic acid anilide) f = plasticizers S = lavender perfume h = trichloroethylphosphate .

Claims (20)

4. C L A I M S

1. A process for the production of microcapsules in which a reaction product of a .diol or polyol with phosgene or a diisocyanate or polyisocyanate , which reaction product contains at least two a, chloroformic acid ester or isocyante groups per molecule, is mixed with the. material which is to be encapsulated and the resulting mixture, together with a chain-lengthening agent which is at least bifunctional and an aqueous phase, is introduced into a zone of high turbulence in which the reaction product and the chain-lengthening agent react together to form a high molecular weight polymer which envelops the core material to form microcapsules and the microcapsules are then separated.

2. A process as claimed in claim 1 in which the diol or polyol has a molecular, weight of from 400 to 10,000.

3. A process as claimed in claim 2 in which the diol or polyol has a molecular weight of from 1 ,000 to 10,000.

4. A process as claimed in any of claims 1 to 3 in which the · polyol contains from 2 to 8 hydroxyl groups per molecule.

5. A process as claimed in any of claims 1 to 3 in which the polyol is a polyester, polyether, polythloether, polyacetal, polycarbonate or polyester amide.

6. A process as claimed in any of claims 1 to 5 in which the molar ratio of *f isocyanate or chloroformic acid ester groups to active hydrogen in the chain-lengthening agent is between 1 :0.8 and 1:1.8.

7. A process as claimed in claim 6 in which the molar ratio, of isocyanate or chloroformic acid ester groups to active hydrogen in the chain lengthening agent is 1:1.

8. A process as claimed in any of claims .1 to 7 in which the reaction mixture further a catalyst for urethane formation.

9. A process as claimed in claim 8 in which the quantity of A.

10. A process as claimed in. any of claims 1 to 9 in which the aqueous phase is water or an aqueous emulsifier solution.

11. . A process as claimed in claim 1 0 in which the emulsifier is used in a quantity of from 0. 1 to 1# by weight.

12. 1 2 . A process as claimed in any of claims 1 to 1 1 in which the quantity of aqueous phase is from 50 to 80$ by weight, based on the prepolymer.

13. 1 3 . A process as claimed in .any of claims 1 to 1 2 in which the substance to be encapsulated is dissolved or dispersed in the prepolymer, in a. concentration of up to 90$ by weight, based on the prepolymer.

14. A process as claimed in claim.1 3 in which the substance which is to be encapsulated is dissolved or dispersed in the prepolymer in a concentration of from 20 to 60# by weight.

15. 1 5 . A process as claimed in any of claims to 1 4 in which the; encapsulation is carried out at a temperature of from 50 to 1 50°C

16. 1 6. A process as claimed in any of claims.1 to 1 5 in which at least 300 parts by volume of liquid are passed through per unit volume per hour of the turbulent zone..

17. 1 7. A process as claimed in. claim 1 6 which the throughput of liquid is from 1 200. to 5400 parts by volume of liquid per unit volume per hour of the turbulent zone.

18. I A process as claimed in claim 1 substantially as herein described with reference to the Examples ,

19. 1 9. A process as claimed in claim 1 substantially as herein described with reference to any one of the accompanying drawings.

20. Microcapsules when prepared by a process as claimed in any of claims 1 to 1 9-.- I Le A 1 28